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Cross-coupling reactions desymmetrizing

The enantioselective desymmetrization strategy can also be used for the palladium-catalyzed cross-coupling reactions with Grignard reagents. Thus, in the... [Pg.95]

The requisite dihydroxyketones are commonly assembled via iterative aldol coupling reactions [1], but other methods including Nef reactions [17,18], acetylide additions [19, 20], 1,3-dipolar nitrile oxide cycloadditions [21], iterative alkylation of dithianes [22-28], hydrazones [29], oximes [30], nitriles [31], or dihalomethylene species [32-34], cross-metathesis/hydroboration/oxidation [35], iterative substitution of a xanthate [36], dihydroxylation/desymmetrization of alkenes [37], Homer-Wadsworth-Emmons olehnations [38, 39], allylmetallations [40], and alkyne-alkyne cross-coupling [41] have also been reported. [Pg.193]


See other pages where Cross-coupling reactions desymmetrizing is mentioned: [Pg.305]    [Pg.307]    [Pg.477]    [Pg.307]    [Pg.462]    [Pg.305]    [Pg.147]    [Pg.470]    [Pg.178]    [Pg.887]    [Pg.261]   
See also in sourсe #XX -- [ Pg.305 ]




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